2001
DOI: 10.1002/1520-6017(200103)90:3<253::aid-jps1>3.3.co;2-n
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Oxidative degradation of pharmaceuticals: Theory, mechanisms and inhibition

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Cited by 65 publications
(102 citation statements)
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“…The HCl, NaOH, NH2OH and H2O2 at appropriate concentration were evaluated as degradation agents for cleaning or decontamination. 6 Permanganate ion oxidizes a larger variety of substrate and finds extensive application in organic synthesis. [7][8][9][10][11][12] During oxidation permanganate is reduced to various oxidation states in acidic, alkaline and neutral media.…”
Section: Introductionmentioning
confidence: 99%
“…The HCl, NaOH, NH2OH and H2O2 at appropriate concentration were evaluated as degradation agents for cleaning or decontamination. 6 Permanganate ion oxidizes a larger variety of substrate and finds extensive application in organic synthesis. [7][8][9][10][11][12] During oxidation permanganate is reduced to various oxidation states in acidic, alkaline and neutral media.…”
Section: Introductionmentioning
confidence: 99%
“…Oxidation is common in pharmaceuticals and can proceed through a variety of mechanisms. These include autoxidation and other free radical processes, electron transfer, and nucleophilic or electrophilic reactions of peroxides [17,18]. For cases in which trappable free radicals are present, radicalscavenging antioxidants (e.g., BHA) have been employed to prevent oxidation.…”
Section: Introductionmentioning
confidence: 99%
“…The drug-excipient interaction in formulated dosage forms has been reported in a number of papers. [30][31][32][33][34][35][36][37][38][39][40][41][42][43][44][45][46][47][48] For example, lactose has been widely used as a filler or diluent in tablets and capsules. Because lactose is a reducing sugar, it can react with a drug substance containing a primary or secondary amine to form degradation products through a well-known Maillard reaction mechanism.…”
Section: Characteristics Of Impurity Identification In Formulation Dementioning
confidence: 99%
“…11,19,36,37 In addition, pharmaceutical impurities may come from a variety of sources and channels, some are even unexpected. Consequently, identification of these unknown impurities in the formulation development is quite challenging.…”
Section: Complexity Of Impurity Identification In Pharmaceutical Dosamentioning
confidence: 99%